Resmed Pty , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Resmed Pty , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Mariana Minerva, AirFit F20 Mask System, S10 Kirra
3
Total
3
Cleared
0
Denied
Resmed Pty , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Bella Vista, AU.
Latest FDA clearance: Feb 2026. Active since 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Resmed Pty , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Resmed Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Resmed Pty , Ltd.
3 devices